Canonical Allele Identifier: CA136837290
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs896002898
gnomAD v2: 6-31327092-G-A
MyVariant Identifiers: chr6:g.31327092G>A (hg19) chr6:g.31359315G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31359315G>A , CM000668.2:g.31359315G>A GRCh38
NC_000006.11:g.31327092G>A , CM000668.1:g.31327092G>A GRCh37
NC_000006.10:g.31435071G>A NCBI36
NG_023187.1:g.2898C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1271-1634C>T
ENST00000481849.6:n.1271-1634C>T
ENST00000497377.6:n.1271-1634C>T
ENST00000696559.1:c.-203-1634C>T ENSP00000512717.1:n.-203-1634C>T
ENST00000696560.1:c.-203-1634C>T ENSP00000512718.1:n.-203-1634C>T
ENST00000696561.1:c.-203-1634C>T ENSP00000512719.1:n.-203-1634C>T
ENST00000696562.1:c.-135-2022C>T ENSP00000512720.1:n.-135-2022C>T
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